Gene domain-specific DNA methylation episignatures highlight distinct molecular entities of ADNP syndrome
Eric G. Bend(Howard Hughes Medical Institute), Bekim Sadiković(Western University), David B. Everman(Greenwood Genetic Center), Michael J. Lyons, Laurie Demmer(Carolinas Medical Center), Sara Cathey(Greenwood Genetic Center), Michael J. Friez(Greenwood Genetic Center), Erfan Aref‐Eshghi(London Health Sciences Centre), Jennifer Kerkhof(London Health Sciences Centre), Alan Stuart(London Health Sciences Centre), Roger E. Stevenson(Piedmont Technical College), Karen W. Gripp(Alfred I. duPont Hospital for Children), Charles E. Schwartz(Greenwood Genetic Center), Michael A. Levy(Western University), Paul R. Mark(Spectrum Health), Håkon Håkonarson(Children's Hospital of Philadelphia), Elizabeth Bhoj(Children's Hospital of Philadelphia), Dong Li(Children's Hospital of Philadelphia), R. Curtis Rogers(Greenwood Genetic Center), Katie Clarkson(Greenwood Genetic Center), Heather L. Davis(Torbay Hospital), Elaine H. Zackai(Children's Hospital of Philadelphia), David I. Rodenhiser(Western University), Eloise J. Prijoles(Greenwood Genetic Center)
Cited by 129
Related Papers
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study
|The Lancet|2015|776
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes
|Nature Genetics|2012|752
<i>AGTR2</i> Mutations in X-Linked Mental Retardation
|Science|2002|719
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures
|Nature Genetics|2008|591